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EuropeTraining

Basics in Clinical Research

general overview of the drug development process

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Who should attend?

Designed for those with little or no experience in clinical research or those seeking an overview of the clinical research process, regulations, terminology, acronyms, roles and responsibilities within clinical research. It is aimed at Clinical Research Assistants, support staff and persons with related functions (eg. IT Support Staff).

Details

The course offers a general overview of the drug development process and most relevant tasks and responsibilities within the clinical research setting, focusing on practical aspects and mainly addressing the needs of assistants and support personnel

It provides details on how drugs are developed, who the key players in the process are, terminology used, essential rules, guidelines and laws as well as information on clinical studies and documentation required in clinical research.

 

Prices

Early Bird Fee: CHF 990.00 + 7.7% VAT (valid until: 09.10.2019) Regular Fee: CHF 1'100.00 + 7.7% VAT (valid after: 09.10.2019) 10 % reduction for CTC employees, SwAPP and SBA members. For special fees and group discounts, please contact: training@ctcresourcing.com

Contact

Tamara Kohler
tamara.kohler@ctcresourcing.com

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